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Documenti fondamentali

11709

Supelco

Barbituric acid

for spectrophotometric det. of cyanide, ≥99.5%

Sinonimo/i:

2,4,6-Trihydroxypyrimidine, Malonylurea

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About This Item

Formula empirica (notazione di Hill):
C4H4N2O3
Numero CAS:
Peso molecolare:
128.09
Beilstein:
120502
Numero CE:
Numero MDL:
Codice UNSPSC:
12000000
ID PubChem:
NACRES:
NA.21

Livello qualitativo

Saggio

≥99.5% (HPLC)
≥99.5%

Stato

solid

Qualità

for spectrophotometric det. of cyanide

tecniche

UV/Vis spectroscopy: suitable

Residuo alla calcinazione

≤0.05%

Punto di fusione

248-252 °C (dec.) (lit.)

Anioni in tracce

chloride (Cl-): ≤50 mg/kg
sulfate (SO42-): ≤500 mg/kg

Cationi in tracce

Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
Mg: ≤10 mg/kg
Mn: ≤5 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

Stringa SMILE

O=C1CC(=O)NC(=O)N1

InChI

1S/C4H4N2O3/c7-2-1-3(8)6-4(9)5-2/h1H2,(H2,5,6,7,8,9)
HNYOPLTXPVRDBG-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Barbituric acid is also known as malonurea or 6-hydroxyuracil, it is an odourless powder and is soluble in water. It has a very high pharmacological activity and can be used to synthesize addition derivatives of it, to be used in novel drug discovery. It basically acts on the central nervous system (CNS) depressants, thereby possessing a wide range from mild sedation to total anaesthesia.

Applicazioni

Barbituric acid with aromatic aldehydes was used in an experimental study, meant to demonstrate the increased efficiency of Knoevenagel condensation reaction for barbituric acid and various aromatic aldehydes on basic alumina, in the absence of organic solvents under microwave irradiation. It may also be used in electrochemical oxidation of iodine, using cyclic voltammetry and controlled-potential coulometry.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

302.0 °F - closed cup

Punto d’infiammabilità (°C)

150.00 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Succinimide

Electrochemical study of iodide in the presence of barbituric acid. Application to coulometric titration of barbituric acid.
Nematollahi D and Hesari M
Microchemical Journal, Devoted to the Application of Microtechniques in All Branches of Science, 70 (1), 7-11 (2001)
Microwave enhanced knoevenagel condensation of barbituric acid with aromatic aldehydes on basic alumina.
Khalafi NA and Hashemi A.
Iranian Journal of Chemistry and Chemical Engineering, 20 (1), 9-11 (2001)
Bioactive Heterocyclic Compound Classes.
Clemens L and Dinges J.
Pharmaceutics, 24-27 (2012)
Sergio Hidalgo-Figueroa et al.
Chemical biology & drug design, 81(4), 474-483 (2013-01-08)
A small series of thiazolidine-2,4-dione and barbituric acid derivatives 1-4 was prepared using a short synthetic route, and all compounds were characterized by elemental analysis, mass spectrometry, and NMR ((1)H, (13)C) spectroscopy. Their in vitro relative expression of peroxisome proliferator-activated
David C Chiara et al.
The Journal of biological chemistry, 288(27), 19343-19357 (2013-05-17)
GABA type A receptors (GABAAR), the brain's major inhibitory neurotransmitter receptors, are the targets for many general anesthetics, including volatile anesthetics, etomidate, propofol, and barbiturates. How such structurally diverse agents can act similarly as positive allosteric modulators of GABAARs remains

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